Canonical Allele Identifier: CA409806349

Gene: APP

Linked Data

• MyVariant Identifiers: chr21:g.27269916T>A (hg19) ; chr21:g.25897604T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.25897604T>A , CM000683.2:g.25897604T>A	GRCh38
NC_000021.8:g.27269916T>A , CM000683.1:g.27269916T>A	GRCh37
NC_000021.7:g.26191787T>A	NCBI36
NG_007376.1:g.278217A>T
NG_007376.2:g.278525A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000707132.1:n.2000A>T
ENST00000707133.1:n.430A>T
ENST00000707134.1:n.699A>T
ENST00000346798.8:c.2033A>T MANE Select	ENSP00000284981.4:p.Asp678Val
ENST00000346798.7:c.2033A>T	ENSP00000284981.4:p.Asp678Val
ENST00000348990.9:c.1808A>T	ENSP00000345463.5:p.Asp603Val
ENST00000354192.7:c.1640A>T	ENSP00000346129.3:p.Asp547Val
ENST00000357903.7:c.1976A>T	ENSP00000350578.3:p.Asp659Val
ENST00000358918.7:c.1979A>T	ENSP00000351796.3:p.Asp660Val
ENST00000359726.7:c.1703A>T	ENSP00000352760.4:p.Asp568Val
ENST00000439274.6:c.1865A>T	ENSP00000398879.2:p.Asp622Val
ENST00000440126.7:c.1961A>T	ENSP00000387483.2:p.Asp654Val
ENST00000464867.1:n.380A>T
NM_000484.3:c.2033A>T	NP_000475.1:p.Asp678Val
NM_001136016.3:c.1961A>T	NP_001129488.1:p.Asp654Val
NM_001136129.2:c.1640A>T	NP_001129601.1:p.Asp547Val
NM_001136130.2:c.1865A>T	NP_001129602.1:p.Asp622Val
NM_001136131.2:c.1703A>T	NP_001129603.1:p.Asp568Val
NM_001204301.1:c.1979A>T	NP_001191230.1:p.Asp660Val
NM_001204302.1:c.1922A>T	NP_001191231.1:p.Asp641Val
NM_001204303.1:c.1754A>T	NP_001191232.1:p.Asp585Val
NM_201413.2:c.1976A>T	NP_958816.1:p.Asp659Val
NM_201414.2:c.1808A>T	NP_958817.1:p.Asp603Val
NM_000484.4:c.2033A>T MANE Select	NP_000475.1:p.Asp678Val
NM_001136129.3:c.1640A>T	NP_001129601.1:p.Asp547Val
NM_001136130.3:c.1865A>T	NP_001129602.1:p.Asp622Val
NM_001204301.2:c.1979A>T	NP_001191230.1:p.Asp660Val
NM_001204302.2:c.1922A>T	NP_001191231.1:p.Asp641Val
NM_001204303.2:c.1754A>T	NP_001191232.1:p.Asp585Val
NM_201413.3:c.1976A>T	NP_958816.1:p.Asp659Val
NM_201414.3:c.1808A>T	NP_958817.1:p.Asp603Val
NM_001136131.3:c.1703A>T	NP_001129603.1:p.Asp568Val
NM_001385253.1:c.1865A>T	NP_001372182.1:p.Asp622Val